Manifold reduction of moesin in fetal Down syndrome brain

被引:18
作者
Lubec, B
Weitzdoerfer, R
Fountoulakis, M
机构
[1] Univ Vienna, Dept Neonatol, A-1090 Vienna, Austria
[2] F Hoffmann La Roche & Co Ltd, Pharmaceut Res, Gene Technol, CH-4070 Basel, Switzerland
关键词
Down syndrome; ERM family; ezrin; fetal; moesin; radixin; trisomy; 21;
D O I
10.1006/bbrc.2001.5520
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Moesin is a member of the ERM family and is involved in plasma membrane-actin cytoskeleton crosslinking, resulting cell adhesion, shape, and motility. Because moesin was shown to be highly expressed in growth cones and moesin/radixin suppression led to impaired structure and function of this key element in brain development, we tested the ERM family, ezrin, radixin, and moesin, in fetal Down syndrome (DS) cortex at the early second trimester. We applied two-dimensional gel electrophoresis with subsequent MALDI detection and identification of protein spots followed by quantification with specific software. Moesin was shown to be significantly and manifold reduced in fetal DS brain, whereas reduction of ezrin and radixin did not reach statistical significance. We therefore propose the involvement of moesin in developmental impairment of DS brain, including deteriorated arborisation, neuritic outgrowth, and neuronal migration. Furthermore, decreased moesin is the second F-actin bundling protein, besides drebrin, that is manifold reduced in fetal DS brain. (C) 2001 Academic Press.
引用
收藏
页码:1191 / 1194
页数:4
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